Myo-Tronics Research, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Myo-Tronics Research, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Myo-Tronics Research, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1977 to 1984. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Myo-Tronics Research, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Myo-Tronics Research, Inc.
8 devices
Cleared
Nov 19, 1984
J4 MYO-MONITOR
Dental
167d
Cleared
Nov 19, 1984
BNS 40
Dental
167d
Cleared
Feb 10, 1984
MUCOSAL ADJUSTMENT PASTE LIQUID SPRAY
Dental
150d
Cleared
May 27, 1983
TESTCORP RA
Microbiology
31d
Cleared
Feb 09, 1983
MODEL EM-2 BIOELECTRIC PROCESSOR
Dental
33d
Cleared
Mar 05, 1982
ELECTRIC MUSCLE STIMULATOR
Physical Medicine
78d
Cleared
Mar 31, 1981
MODEL EM-IR
Dental
33d
Cleared
Feb 18, 1977
MONITOR, MYO, MODEL J3
Dental
9d